Primary Site >> Liver Cancer

Gene >> L1CAM

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000370060
Start 153872664:153872664(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.125C>T
AA Mutation p.Pro42Leu(p.P42L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000370060
Start 153870853:153870853(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs202000092
CDS Mutation c.631G>T
AA Mutation p.Ala211Ser(p.A211S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000370060
Start 153870398:153870398(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.796G>A
AA Mutation p.Ala266Thr(p.A266T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000370060
Start 153863486:153863486(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3521G>T
AA Mutation p.Gly1174Val(p.G1174V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000370060
Start 153868006:153868006(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1820T>C
AA Mutation p.Leu607Ser(p.L607S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000370060
Start 153870234:153870234(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.813G>T
Mutation Classification Silent
Feature Type Transcript